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Identification of a myometrial molecular profile for dystocic labor
© Brennan et al; licensee BioMed Central Ltd. 2011
Received: 11 August 2011
Accepted: 16 October 2011
Published: 16 October 2011
The most common indication for cesarean section (CS) in nulliparous women is dystocia secondary to ineffective myometrial contractility. The aim of this study was to identify a molecular profile in myometrium associated with dystocic labor.
Myometrial biopsies were obtained from the upper incisional margins of nulliparous women undergoing lower segment CS for dystocia (n = 4) and control women undergoing CS in the second stage who had demonstrated efficient uterine action during the first stage of labor (n = 4). All patients were in spontaneous (non-induced) labor and had received intrapartum oxytocin to accelerate labor. RNA was extracted from biopsies and hybridized to Affymetrix HuGene U133A Plus 2 microarrays. Internal validation was performed using quantitative SYBR Green Real-Time PCR.
Seventy genes were differentially expressed between the two groups. 58 genes were down-regulated in the dystocia group. Gene ontology analysis revealed 12 of the 58 down-regulated genes were involved in the immune response. These included (ERAP2, (8.67 fold change (FC)) HLA-DQB1 (7.88 FC) CD28 (2.60 FC), LILRA3 (2.87 FC) and TGFBR3 (2.1 FC)) Hierarchical clustering demonstrated a difference in global gene expression patterns between the samples from dystocic and non-dystocic labours. RT-PCR validation was performed on 4 genes ERAP2, CD28, LILRA3 and TGFBR3
These findings suggest an underlying molecular basis for dystocia in nulliparous women in spontaneous labor. Differentially expressed genes suggest an important role for the immune response in dystocic labor and may provide important indicators for new diagnostic assays and potential intrapartum therapeutic targets.
As cesarean section (CS) rates continue to rise throughout the developed world, an improved understanding of the molecular mechanisms underlying parturition at term is urgently required. Between 1974 and 2008 overall cesarean rates increased from 5% to 19.1% in the National Maternity Hospital (NMH), Dublin and one of the major contributors to this was a 4-fold increase in cesarean deliveries amongst term singleton cephalic nulliparas (TSCN) . CS rates vary between institutions, although TSCN CS rates correlate with institutional CS rates and we have previously documented that 98% of inter-institutional variation in overall CS rates can be attributed to TSCN rates , which demonstrates that TSCN as a cohort has a significant impact on cesarean rates within any obstetric population. However, despite much attention within the obstetric literature addressing the timing and mode of twin deliveries , vaginal breech delivery  and the optimum management of pre-term, growth-restricted fetuses , little emphasis has been placed on the management of TSCN, an important group of parturients, which has been relatively neglected hitherto by research initiatives .
The most common primary indication for CS is dystocia or slow labor, most commonly secondary to inefficient myometrial contractility. Dystocia is a common obstetric problem, affecting 3-8% of deliveries , and is a particular complication of first pregnancies. In approximately 40% of first labors, dystocia can be adequately and safely corrected by intrapartum administration of oxytocin, resulting in vaginal delivery . In 10-20% of cases of dystocia, however, myometrial response to oxytocin is poor and CS becomes the only safe option following prolonged labor . It is believed this complication is likely to increase mainly due to delayed childbearing and increased prevalence of obesity in the obstetric population both factors which adversely affect intrapartum myometrial contractility [9, 10]. For every 1% increase in the incidence of nulliparous CS for dystocia, overall caesarean rates will inevitably increase by at least 0.5% due to the consequent increase in CS in women with scarred uteri. An improved understanding of the molecular mechanisms underlying dystocic labor and may result in alternative adjuvants to oxytocin.
To date, we are not aware of studies using gene expression profiling to evaluate the physiology and mechanisms underlying dystocia in nulliparous women in spontaneous labor. In a large Swedish population-based study, which examined over two million deliveries, Algovik et al demonstrated a large genetic influence on dystocia . This study estimated that heritability contributed 28% in the liability of developing primary dystocia, with significant concordance evident amongst monozygotic twins and an increased risk of dystocia in women who had a mother or sister with a history of dystocic labors. Additionally, transgenic knockout mouse models examining prostaglandin F2α receptor  and testosterone 5-α-reductase type 1 , respectively, exhibit an absence of parturition, although screening for mutations in these candidate dystocia-related genes in humans proved unsuccessful . The genetic basis of dystocia is likely to be more complex that a single gene mutation. Considering the clinical impact of dystocia, a single gene mutation would be subject to purifying selection and would be selected against in the evolutionary process. Therefore genome-wide screening should provide more useful insights. The aim of this study was to use gene expression microarrays to examine the temporal and spatial changes in myometrial gene expression during normally-progressing and dystocic labors to improve our understanding of the molecular mechanisms underlying term dystocic labor.
Definitions used for this study included: nulliparous: para 0, irrespective of gravidity; term: greater than or equal to 37 completed weeks gestation and singleton gestation, no evidence of a multiple gestation after the first trimester. Representative partograms for both groups used in this study are shown in Figure 1.
Myometrial samples were transferred directly in the operating room into RNALater (Qiagen, Crawley, West Sussex, UK) and stored at 4°C for 24 hours. RNALater was then removed and samples were stored at -80°C. Total RNA extraction and purification from tissue samples were carried out using TRIzol reagent (Invitrogen, Carlsbad, CA) as per the manufacturer's protocol. Preparation of labeled complementary RNA and hybridization to HGU133 Plus 2.0 GeneChips (Affymetrix, Santa Clara, CA) was performed as per the manufacturer's recommended protocol.
Raw data (cel files) were analyzed using Bioconductor 1.9 http://bioconductor.org running on R 2.6.0 . Normalization was performed using the Affymetrix package's Robust Multichip Average (RMA) default method . Differential gene expression was measured using a modified t test, and genes demonstrating greater than 2 fold difference and a p value < 0.05 were considered to be differentially expressed. Hierarchical clustering and principal components analysis were performed using MatLab 7 (MathWorks, Apple Hill Drive, MA). Raw data are available in Geo http://www.ncbi.nlm.nih.gov/projects/geo/, accession number GSE32178.
Quantitative SYBR Green Real-Time PCR
Total RNA was isolated from tissues using Trizol (Invitrogen) and reverse transcribed using SuperScript II™ Reverse Transcriptase (Invitrogen) according to the manufacturer's instructions. ERAP2 (FW-TGGATGGGACCAACTCATTACA, RV- TGCACCAACTAGCTGAAACAC), CD28 (FW- GGCATCCCTTCACAAAGGACT, RV- CCCCGTTTTTGAGTAAACCTGA), LILRA3 (FW- CCAGTGTGTTTCTGATGTCAGC, RV- CCGGATGCACCGAGATGAAG), HLA-DQB1 (FW- AGGGTGAATGTTTCCCCCTC, RV- CTGCCTGGGTAGAAATCCGT) primers were designed using Primer Express software (Applied Biosystems Version 2.0) and used to amplify specific DNA fragments with SYBR Green PCR Master Mix (Applied Biosystems) using a 7900HT Fast Real-Time PCR System (Applied Biosystems). Relative expression levels were calculated using the qBase real-time PCR relative quantification software  with all samples normalized to GAPDH expression. Negative controls included a no template control and a no reverse transcriptase control. All qRT-PCR reactions were performed in triplicate.
Genome-wide transcriptomic analysis was performed on myometrial biopsies taken from the lower uterine segment in Caucasian women undergoing CS for dystocia (n = 4) and in women who demonstrated efficient uterine action in the first stage of labor, but underwent a second stage CS for persistent occiput posterior position. All of the patients included in the study were nulliparas in spontaneous labor between 37 and 42 weeks. There were no differences between the two groups regarding maternal age, BMI, or gestation at delivery (Table 1). The mean birthweight in the dystocic group was 3667 gm compared to 3839 gm in the efficient uterine action group; all patients received epidural anaesthesia.
Differentially expressed genes in dystocic labor
endoplasmic reticulum aminopeptidase 2
chromosome 15 open reading frame 48
major histocompatibility complex, class II, DQ beta 1
hypothetical gene supported by AL713796
hemoglobin, gamma A
hypothetical gene supported by AL713796
inhibitor of DNA binding 2, dominant negative helix-loop-helix protein
complement component 7
leukocyte immunoglobulin-like receptor, subfamily A (without TM domain), member 3
tripartite motif-containing 13
MLF1 interacting protein
denticleless homolog (Drosophila)
FSHD region gene 1 pseudogene
transcription factor CP2-like 1
ribonucleotide reductase M2
ecotropic viral integration site 2A
ELL associated factor 2
zinc finger protein 367
minichromosome maintenance complex component 4
minichromosome maintenance complex component 10
Kruppel-like factor 5 (intestinal)
centromere protein K
cell division cycle 6 homolog (S. cerevisiae)
granzyme H (cathepsin G-like 2, protein h-CCPX)
DEAD (Asp-Glu-Ala-Asp) box polypeptide 17
mitochondrial ribosomal protein L43
hepcidin antimicrobial peptide
minichromosome maintenance complex component 2
GRB2-binding adaptor protein, transmembrane
Ras-related GTP binding D
triggering receptor expressed on myeloid cells 2
PDZ binding kinase
sushi, von Willebrand factor type A, EGF and pentraxin domain containing 1
transforming growth factor, beta receptor III
phosphatidic acid phosphatase type 2A
ubiquitin-like with PHD and ring finger domains 1
transcription factor EC
pleckstrin homology domain containing, family G (with RhoGef domain) member 1
Zwilch, kinetochore associated, homolog (Drosophila)
sperm autoantigenic protein 17
serine/threonine kinase 17b
Fc fragment of IgG, high affinity Ia, receptor (CD64)
MAFF interacting protein
budding uninhibited by benzimidazoles 1 homolog beta (yeast)
ribonucleotide reductase M2
basic helix-loop-helix family, member e41
minichromosome maintenance complex component 5
ATPase, aminophospholipid transporter, class I, type 8B, member 1
ubiquitin-conjugating enzyme E2T (putative)
ATPase family, AAA domain containing 2
oxidation resistance 1
phosphatidic acid phosphatase type 2A
aquaporin 3 (Gill blood group)
MAD2 mitotic arrest deficient-like 1 (yeast)
gypsy retrotransposon integrase 1
regulator of G-protein signaling 17
similar to FRG1 protein (FSHD region gene 1 protein)
integrin beta 3 binding protein (beta3-endonexin)
popeye domain containing 3
Fc fragment of IgG, high affinity Ib, receptor (CD64)
primase, DNA, polypeptide 1 (49kDa)
Although dystocia represents one of the major indications for primary CS, to our knowledge, genome-wide analysis has not been applied to the study of the molecular mechanisms underlying dystocia in term nulliparous labor. High-throughput screening technologies, such as DNA microarrays have been used to improve comprehension of the major structural and metabolic transformations, which affect the myometrium from the very beginning of pregnancy until the onset of labor [18–22]. Changes in the structural and contractile genes associated with the actin cytoskeleton, focal adhesion molecules, adherens and tight junctions represent a large subset of genes that are over-expressed in pregnant, compared to non-pregnant, human myometrium . Additionally, in an attempt to further decipher the causes of pre-term labor, a number of investigators have used transcriptomic approaches to examine the transition from uterine quiescence to the onset of contractions in small numbers of patients [18–22]. These studies identified a number of genes, which may be useful in predicting pre-term labor; however, none have specifically examined dystocia. Our findings demonstrate significant differences in the myometrial transcriptomic profiles of dystocic as compared to normally-progressing labors. In particular, we have demonstrated that a number of key regulators of the host immune response are down-regulated in dystocia.
The strengths of this study are mainly based around the study design whereby the inclusion criteria were strict. Patients included in this study were nulliparas in spontaneous labor. All women in the dystocia group received 30mU/min oxytocin for at least 4 hours. In addition the study was performed in a unit where the diagnosis and management of spontaneous nulliparous labor has been standardized for the last four decades . A major weakness of this study is the small number of samples studied. In addition, sampling the lower segment alone may give a true global description of the dystocic transcriptome. Transcriptomic profiling has shown different myometrial gene expression patterns in lower segment compared to fundal biopsies in labour [22, 23], however the majority of these studies appear to have been performed in multiparous patients and thus these finds may not be applicable to our study. Dystocia, due to ineffective myometrial contractility is much more common in women undergoing induction of labor, although induced labors were specifically excluded from this study in an attempt to compare two homogenous groups. Also the indication for induction is important as a woman undergoing labor induction following a prolonged interval of ruptured membranes is likely to have a different myometrial profile to a patient being induced for pre-eclampsia. The absence of an independent validation cohort represents another weakness of this study, although internal validation using rt-PCR was performed to address this issue.
This study further strengthens the potential argument for an underlying genetic predisposition for dystocia [6, 24]. The finding that the majority of differentially expressed genes were down-regulated suggests that many of these may harbour loss-of-function mutations. The association of dystocia with an impaired immune response is also in agreement with a larger recent study by Mittal et al , who demonstrated increased expression of a number of inflammatory genes in patients with arrest of descent in the second stage, a cohort similar to the efficient uterine action group in our study. Comparison of our findings to those of Mittal et al  should be tempered by the fact that their study did not stratify for parity or mode of onset of labor. The importance of the inflammatory response in spontaneous labor cannot be overstated, since Unal et al  recently demonstrated that maternal inflammatory markers increase before the onset of spontaneous labor, suggesting that any future studies of dystocia should be stratified according to labor onset (spontaneous versus induced). Similarly, dystocia in a multiparous woman is much more likely to be secondary to obstruction than inefficient uterine action and thus likely to have a different underlying molecular profile, emphasizing the need for stratification by parity.
The identification of ERAP2 as a gene that was significantly down-regulated in dystocia is of particular interest because ERAP2 has been identified as a genetic susceptibility locus for preeclampsia in a number of different populations [27, 28]. Although ERAP2 is considered to be a member of the oxytocinase subfamily of M1 aminopeptidases, it has no hydrolytic activity towards oxytocin . ERAP2 which is regulated by interferon gamma appears to play a key role in the innate immune response whereby it trims various N-terminal extended precursors to major histocompatibility complex class I-presented antigenic peptides . Although a number of missense single nucleotide polymorphisms (SNP) in ERAP2 have been associated with an increased risk of preeclampsia [27, 28], the functional importance of these SNPs is still not fully understood. A recent study did however demonstrate that specific ERAP2 haplotypes are associated with lower levels of MHC class I expressed on the surface of B cells, suggesting that naturally occurring ERAP2 deficiency affects MHC presentation and immune response .
Although historical studies have suggested that labor may be easier to induce in preeclamptic patients [31, 32], a number of recent reports have suggested that women with preeclampsia undergoing labor induction have higher cesarean delivery rates compared with non-preeclamptics, independent of parity or gestational age [33–35]. In a large retrospective cohort study, Kim et al demonstrated a significantly higher term nulliparous CS rate in induced preeclamptic patients compared to healthy controls . While our study was conducted on nulliparas in spontaneous term labour these findings raise intriguing questions about the role of ERAP2 and efficient uterine action in preeclamptic patients, which warrant further investigation.
Our study demonstrates an obvious difference in the myometrial transcriptomic profiles in women with dystocia and efficient uterine action but it also raises a number of questions. It is currently not possible to predict which women will develop dystocia before the onset of spontaneous labor. Due to the invasive nature of a biopsy, it would not be possible to reduce a myometrial profile to clinical utility, but it is worth noting that two of the genes significantly down-regulated in dystocic patients, ERAP2 and LILRA3, code for secreted proteins which could potentially be detected in human plasma. LILRA3 has previously been detected in rheumatoid arthritis . Nevertheless, the advent of whole genome sequencing offers a platform to further investigate dystocia and to identify the genetic determinants of this complex condition, which is central to ever-increasing international CS rates and thus represents a major current public health issue.
DJB, MR and COH are obstetricians and gynaecologists. DJB, SMG, ER and DOC are research scientists with an interest in biomarker identification and validation
The study was funded by the National Maternity Hospital Research Fund
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